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Deuterium Labeled Compounds

Deuterium Labeled Compounds

氘(氢-2)标记化合物是其中一个或多个氢原子被氘(氢的稳定同位素)取代的化合物。氘的原子核中有一个质子和一个中子,而最常见的氢同位素(氕)只有一个质子。氘(氢-2)标记化合物可用于研究药物代谢和反应动力学。
TargetMol isotope
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Cat. No. Product Name CAS No. Purity Chemical Structure
T10663 Calcitriol-d6
骨化三醇 D6
78782-99-7 98%
TargetMol Chemical Structure Calcitriol-d6
Calcitriol D6 is the deuterated form of Calcitriol, which is the hormonally active form of vitamin D. Calcitriol is the active metabolite of vitamin D3 that acti...
T12144 N-Desethyl Oxybutynin-d5 hydrochloride
化合物 T12144
1173018-49-9 98%
TargetMol Chemical Structure N-Desethyl Oxybutynin-d5 hydrochloride
N-Desethyl Oxybutynin D5 hydrochloride is the the active metabolite Oxybutynin, is deuterium labeled N-Desethyl Oxybutynin hydrochloride.
T29867 ALK-001
化合物 T29867
118139-36-9 98%
TargetMol Chemical Structure ALK-001
ALK-001 is a vitamin A analog, which may be used to treat Stargardt disease.
T71286 Guaifenesin-d3
化合物 Guaifenesin-d3
1189924-85-3 98%
TargetMol Chemical Structure Guaifenesin-d3
Guaifenesin-d3 is intended for use as an internal standard for the quantification of guaifenesin by GC- or LC-MS. Guaifenesin is an expectorant. It inhibits prod...
T11639 Imatinib D4
化合物 T11639
1134803-16-9 98%
TargetMol Chemical Structure Imatinib D4
Imatinib D4 is a deuterium-labeled Imatinib. Imatinib is an orally bioavailable tyrosine kinases inhibitor that selectively inhibits BCR/ABL, PDGFR, v-Abl, and ...
T19119 3-Hydroxy Midostaurin-D5
化合物 T19119
98%
TargetMol Chemical Structure 3-Hydroxy Midostaurin-D5
3-Hydroxy Midostaurin-D5 (CGP52421-D5) is a deuterium-labeled 3-Hydroxy Midostaurin which is a metabolite of PKC412. PKC412 effectively inhibits FMS-like tyrosin...
T12355 Palbociclib-d8
化合物 T12355
1628752-83-9 98%
TargetMol Chemical Structure Palbociclib-d8
Palbociclib D8 is a deuterium labeled Palbociclib. Palbociclib is a selective and orally active inhibitor of CDK4 and CDK6 (IC50s of 11 and 16 nM, respectively)....
T69995 Chlorhexidine-d8 HCl
化合物 Chlorhexidine-d8 HCl
2012598-75-1 98%
TargetMol Chemical Structure Chlorhexidine-d8 HCl
Chlorhexidine-d8 is intended for use as an internal standard for the quantification of chlorhexidine by GC- or LC-MS. Chlorhexidine is a bis(biguanide) antimicro...
T12657 (Rac)-Atomoxetine D7 hydrochloride
化合物 T12657
98%
TargetMol Chemical Structure (Rac)-Atomoxetine D7 hydrochloride
(Rac)-Atomoxetine D7 hydrochloride is a deuterium labeled (Rac)-Atomoxetine hydrochloride. (Rac)-Atomoxetine hydrochloride is a racemic form of Atomoxetine hydro...
T13282 Valsartan-d9
缬沙坦 D9
1089736-73-1 98%
TargetMol Chemical Structure Valsartan-d9
Valsartan D9 is a deuterium-labeled valsartan. Valsartan is an antagonist of the angiotensin II receptor and for the treatment of high blood pressure and heart f...
T12167 Nadolol-d9
纳多洛尔 D9
94513-92-5 98%
TargetMol Chemical Structure Nadolol-d9
Nadolol D9 is the deuterium labeled Nadolol is a blocker of non-selective beta.
T10351 Aprocitentan D4
化合物 T10351
98%
TargetMol Chemical Structure Aprocitentan D4
Aprocitentan D4 (ACT-132577 D4) is a deuterium-labeled Aprocitentan. Aprocitentan is a major and pharmacologically active metabolite of Macitentan. Aprocitentan ...
T10279 Alfacalcidol-D6
化合物 T10279
1641940-94-4 98%
TargetMol Chemical Structure Alfacalcidol-D6
Alfacalcidol-D6 is a deuterated Alfacalcidol. Alfacalcidol is a non-selective VDR activator medication.
T34590 SD-254
化合物 T34590
940297-30-3 98%
TargetMol Chemical Structure SD-254
SD-254 is a deuterium analog of Effexor, with fewer side effects and a longer half-life.
T12476 Pimozide-d4
化合物 T12476
1803193-57-8 98%
TargetMol Chemical Structure Pimozide-d4
Pimozide D4 is a deuterium labeled Pimozide.
T10284 ALK-IN-6
化合物 T10284
2055821-33-3 98%
TargetMol Chemical Structure ALK-IN-6
ALK-IN-6 is an orally bioavailable inhibitor of anaplastic lymphoma kinase (ALK, IC50s: 71 nM, 18.72 nM, and 36.81 nM for ALK wild, ALK F1196M and ALK F1174L).
T70960 Maprotiline-d3 hydrochloride
化合物 Maprotiline-d3 hydrochloride
1329496-63-0 98%
TargetMol Chemical Structure Maprotiline-d3 hydrochloride
Maprotiline-d3 is intended for use as an internal standard for the quantification of maprotiline by GC- or LC-MS. Maprotiline is a tricyclic antidepressant. It b...
T71305 Clofibric Acid-d4
化合物 Clofibric Acid-d4
1184991-14-7 98%
TargetMol Chemical Structure Clofibric Acid-d4
Clofibric acid-d4 is intended for use as an internal standard for the quantification of clofibric acid by GC- or LC-MS. Clofibric acid is a peroxisome proliferat...
T13195 Trandolapril D5
化合物 T13195
1356847-98-7 98%
TargetMol Chemical Structure Trandolapril D5
Trandolapril D5 is a deuterium labeled Trandolapril. Trandolapril is an orally active inhibitor of angiotensin converting enzyme (ACE) for hypertension and conge...
T19305 Eldecalcitol-d6
化合物 T19305
98%
TargetMol Chemical Structure Eldecalcitol-d6
Eldecalcitol is an orally active analogue of active vitamin D used in the treatment of osteoporosis. Eldecalcitol-d6 is the deuterium labeled Eldecalcitol.
Calcitriol-d6
T10663
Calcitriol D6 is the deuterated form of Calcitriol, which is the hormonally active form of vitamin D. Calcitriol is the active metabolite of vitamin D3 that acti...
N-Desethyl Oxybutynin-d5 hydrochloride
T12144
N-Desethyl Oxybutynin D5 hydrochloride is the the active metabolite Oxybutynin, is deuterium labeled N-Desethyl Oxybutynin hydrochloride.
ALK-001
T29867
ALK-001 is a vitamin A analog, which may be used to treat Stargardt disease.
Guaifenesin-d3
T71286
Guaifenesin-d3 is intended for use as an internal standard for the quantification of guaifenesin by GC- or LC-MS. Guaifenesin is an expectorant. It inhibits prod...
Imatinib D4
T11639
Imatinib D4 is a deuterium-labeled Imatinib. Imatinib is an orally bioavailable tyrosine kinases inhibitor that selectively inhibits BCR/ABL, PDGFR, v-Abl, and ...
3-Hydroxy Midostaurin-D5
T19119
3-Hydroxy Midostaurin-D5 (CGP52421-D5) is a deuterium-labeled 3-Hydroxy Midostaurin which is a metabolite of PKC412. PKC412 effectively inhibits FMS-like tyrosin...
Palbociclib-d8
T12355
Palbociclib D8 is a deuterium labeled Palbociclib. Palbociclib is a selective and orally active inhibitor of CDK4 and CDK6 (IC50s of 11 and 16 nM, respectively)....
Chlorhexidine-d8 HCl
T69995
Chlorhexidine-d8 is intended for use as an internal standard for the quantification of chlorhexidine by GC- or LC-MS. Chlorhexidine is a bis(biguanide) antimicro...
(Rac)-Atomoxetine D7 hydrochloride
T12657
(Rac)-Atomoxetine D7 hydrochloride is a deuterium labeled (Rac)-Atomoxetine hydrochloride. (Rac)-Atomoxetine hydrochloride is a racemic form of Atomoxetine hydro...
Valsartan-d9
T13282
Valsartan D9 is a deuterium-labeled valsartan. Valsartan is an antagonist of the angiotensin II receptor and for the treatment of high blood pressure and heart f...
Nadolol-d9
T12167
Nadolol D9 is the deuterium labeled Nadolol is a blocker of non-selective beta.
Aprocitentan D4
T10351
Aprocitentan D4 (ACT-132577 D4) is a deuterium-labeled Aprocitentan. Aprocitentan is a major and pharmacologically active metabolite of Macitentan. Aprocitentan ...
Alfacalcidol-D6
T10279
Alfacalcidol-D6 is a deuterated Alfacalcidol. Alfacalcidol is a non-selective VDR activator medication.
SD-254
T34590
SD-254 is a deuterium analog of Effexor, with fewer side effects and a longer half-life.
Pimozide-d4
T12476
Pimozide D4 is a deuterium labeled Pimozide.
ALK-IN-6
T10284
ALK-IN-6 is an orally bioavailable inhibitor of anaplastic lymphoma kinase (ALK, IC50s: 71 nM, 18.72 nM, and 36.81 nM for ALK wild, ALK F1196M and ALK F1174L).
Maprotiline-d3 hydrochloride
T70960
Maprotiline-d3 is intended for use as an internal standard for the quantification of maprotiline by GC- or LC-MS. Maprotiline is a tricyclic antidepressant. It b...
Clofibric Acid-d4
T71305
Clofibric acid-d4 is intended for use as an internal standard for the quantification of clofibric acid by GC- or LC-MS. Clofibric acid is a peroxisome proliferat...
Trandolapril D5
T13195
Trandolapril D5 is a deuterium labeled Trandolapril. Trandolapril is an orally active inhibitor of angiotensin converting enzyme (ACE) for hypertension and conge...
Eldecalcitol-d6
T19305
Eldecalcitol is an orally active analogue of active vitamin D used in the treatment of osteoporosis. Eldecalcitol-d6 is the deuterium labeled Eldecalcitol.
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